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All product recalls associated with Aesculap Inc.
Total Recalls
9
Past Year
2
Class I (Serious)
0
Most Recent
Sep 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Possibility of the robotic arm to drop more than 10cm from its original position after pressing the emergency stop button due to failure of the integrated safety mechanism.
The sterile blister packaging may be damaged, and sterility may be compromised.
The sterile blister packaging may be damaged, and sterility may be compromised.
The sterile blister packaging may be damaged, and sterility may be compromised.
The sterile blister packaging may be damaged, and sterility may be compromised.
Needle Holder MB215R was inadvertently distributed as MB362R. Similarly, MB362R was distributed as MB215R during the affected distribution date range. The issue may lead to a short delay in procedure.
Needle Holder MB215R was inadvertently distributed as MB362R. Similarly, MB362R was distributed as MB215R during the affected distribution date range. The issue may lead to a short delay in procedure.